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Use of Introduction Mode to Improve Interactive Voice Response Surveys in Bangladesh and Tanzania

Johns Hopkins Bloomberg School of Public Health logo

Johns Hopkins Bloomberg School of Public Health

Status

Completed

Conditions

Noncommunicable Diseases
Surveys and Questionnaires

Treatments

Other: CATI

Study type

Interventional

Funder types

Other

Identifiers

NCT03772509
00007318-5

Details and patient eligibility

About

This study evaluates the effect of two different introduction modes on interactive voice response (IVR) survey cooperation, response, refusal, and contact rates, in Bangladesh and Tanzania.

Full description

Using random digit dialing (RDD) sampling techniques, participants were randomized to one of two introduction modes, followed by a noncommunicable disease (NCD) risk factor survey. The two modes were computer assisted telephone interview (CATI), in which a call-center employee read the introduction to a participant and received oral consent from them, before sending them the NCD risk factor survey via IVR, or the entire survey, including the introduction and consent, being obtained via IVR. In IVR surveys, participants use their touch tone key pad to answer pre-recorded questions. (i.e. If you are male, press 1; If you are female, press 2). This study was conducted in both Bangladesh and Tanzania.

Enrollment

1,511 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Access to a mobile phone
  • Greater or equal to 18 years of age
  • In Bangladesh, conversant in either English or Bangla language. In Uganda, conversant in either Luo, Luganda, Runyakitara, or English languages.

Exclusion criteria

  • Less than 18 years of age

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

1,511 participants in 2 patient groups

CATI
Experimental group
Description:
Introduction and consent via computer assisted telephone interview
Treatment:
Other: CATI
IVR
No Intervention group
Description:
Introduction and consent via interactive voice response

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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